Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
  • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
  • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
  • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D213/62—Oxygen or sulfur atoms
  • C07D213/63—One oxygen atom
  • C07D213/64—One oxygen atom attached in position 2 or 6
  • C07D213/643—2-Phenoxypyridines; Derivatives thereof
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
  • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings

Definitions

• the said phenyl acetates have the formula ##STR2## wherein R 1 represents hydrogen, cyano, ethynyl or methyl, and
• R 2 and R 3 each represent hydrogen, halogen, C 1 -C 4 -alkyl or C 1 -C 4 -alkoxy.
• Suitable for forming salts are inorganic acids such as HCl, H 2 SO 4 , HBr and H 3 PO 4 , and organic acids such as saturated and unsaturated mono-, di- and tricarboxylic acids, e.g. formic acid, acetic acid, oxalic acid, phthalic acid, succinic acid and citric acid.
• inorganic acids such as HCl, H 2 SO 4 , HBr and H 3 PO 4
• organic acids such as saturated and unsaturated mono-, di- and tricarboxylic acids, e.g. formic acid, acetic acid, oxalic acid, phthalic acid, succinic acid and citric acid.
• halogen denoted by R 2 and R 3 are meant fluorine, chlorine, bromine and iodine, particularly however chlorine.
• alkyl or alkoxy groups in the case of R 2 and R 3 can be straight-chain or branched-chain.
• examples of such groups are, inter alia: methyl, methoxy, ethyl, ethoxy, propyl, propoxy, isopropyl, isopropoxy, n-butyl, n-butoxy and i-, sec- or tert-butyl.
• X represents a halogen atom, especially chlorine or bromine; and in the formula VI, R represents C 1 -C 4 -alkyl, particularly methyl or ethyl.
• Suitable acid-binding agents for the processes 1 and 2 are in particular tertiary amines, such as trialkylamine and pyridine, also hydroxides, oxides, carbonates and bicarbonates of alkali metals and alkaline-earth metals, and also alkali metal alkoholates, e.g. potassium-t.-butylate and sodium methylate.
• the water-binding agent used for the process 3 can be, for example, dicyclohexylcarbodiimide.
• the processes 1 to 4 are performed at a reaction temperature of between -10 and 120° C. generally between 20° and 80° C., at normal or elevated pressure and preferably in an inert solvent or diluent.
• Suitable solvents or diluents are, for example, ethers and ethereal compounds such as diethyl ether, dipropyl ether, dioxane, dimethoxyethane and tetrahydrofuran; amides such as N,N-dialkylated carboxylic acid amides; aliphatic, aromatic and also halogenated hydrocarbons, in particular benzene, toluene, xylene, chloroform and chlorobenzene; nitriles such as acetonitrile; dimethylsulphoxide and ketones such as acetone and methyl ethyl ketone.
• ethers and ethereal compounds such as diethyl ether, dipropyl ether, dioxane, dimethoxyethane and tetrahydrofuran
• amides such as N,N-dialkylated carboxylic acid amides
• the compounds of the formula I are obtained as mixtures of various optically active isomers.
• the different isomeric mixtures can be separated by known methods into the individual isomers.
• ⁇ compound of the formula I ⁇ are meant both the individual isomers and mixtures thereof.
• Suitable additives can be solid or liquid and they correspond to the substances common in formulation practice, such as natural or regenerated substances, solvents, dispersing agents, wetting agents, adhesives, thickeners, binders and/or fertilisers.
• compositions according to the invention are produced in a manner known per se by the intimate mixing and/or grinding of the active substances of the formula I with suitable carriers, optionally with the addition of dispersing agents or solvents which are inert to the active substances.
• suitable carriers optionally with the addition of dispersing agents or solvents which are inert to the active substances.
• the active substances can be obtained and used in the following forms:
• solid preparations dusts, scattering agents, granules (coated granules, impregnated granules and homogeneous granules);
• the content of active substance in the compositions described is between 0.1 and 95%, it is to be mentioned in this respect that with application from an aeroplane, or by other suitable devices, concentrations of up to 99.5% or even the pure active substance can be used.
• the active substances of the formula I can be formulated for example as follows (parts are by weight):
• the active substance is mixed and ground with the carriers.
• the active substance is mixed with epichlorohydrin and dissolved in 6 parts of acetone, and the polyethylene glycol and cetyl polyglycol ether are then added.
• the solution obtained is sprayed onto kaolin and the acetone is subsequently evaporated off in vacuo.
• Emulsions of the concentration required can be prepared from these concentrates by dilution with water.
• Cotton plants were sprayed with a 0.05% aqueous emulsion of the active substance (obtained from a 10% emulsifiable concentrate).

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Life Sciences & Earth Sciences (AREA)
• Agronomy & Crop Science (AREA)
• Pest Control & Pesticides (AREA)
• Plant Pathology (AREA)
• Health & Medical Sciences (AREA)
• Engineering & Computer Science (AREA)
• Dentistry (AREA)
• General Health & Medical Sciences (AREA)
• Wood Science & Technology (AREA)
• Zoology (AREA)
• Environmental Sciences (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)
• Pyridine Compounds (AREA)

Applications Claiming Priority (6)

Publications (1)

Family

ID=27175333

Family Applications (1)

Country Status (13)

Cited By (7)

Families Citing this family (6)

Citations (3)

Family Cites Families (1)

• 1978
  • 1978-07-12 DE DE7878100376T patent/DE2861000D1/de not_active Expired
  • 1978-07-12 EP EP78100376A patent/EP0000508B1/de not_active Expired
  • 1978-07-17 US US05/925,342 patent/US4172135A/en not_active Expired - Lifetime
  • 1978-07-18 NZ NZ187885A patent/NZ187885A/xx unknown
  • 1978-07-18 EG EG451/78A patent/EG13419A/xx active
  • 1978-07-18 CA CA307,598A patent/CA1095052A/en not_active Expired
  • 1978-07-18 IL IL7855162A patent/IL55162A/xx unknown
  • 1978-07-19 AU AU38174/78A patent/AU3817478A/en active Pending
  • 1978-07-19 BR BR7804655A patent/BR7804655A/pt unknown
  • 1978-07-19 GR GR56818A patent/GR72142B/el unknown
  • 1978-07-19 ES ES78471849A patent/ES471849A1/es not_active Expired
  • 1978-07-19 IT IT7825893A patent/IT7825893A0/it unknown
  • 1978-07-20 JP JP8893378A patent/JPS5422374A/ja active Pending

Patent Citations (3)

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